Хайлтын үр дүнгүүд - Azarow, Kenneth
- 10-н 1 - 10 үр дүнгүүдийг харуулж байна
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Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia -н Yu, Lan, Sawle, Ashley D., Wynn, Julia, Aspelund, Gudrun, Stolar, Charles J., Arkovitz, Marc S., Potoka, Douglas, Azarow, Kenneth S., Mychaliska, George B., Shen, Yufeng, Chung, Wendy K.
Хэвлэсэн 2015текст -
2
The association between congenital diaphragmatic hernia and undescended testes -н Azarow, Kenneth S, Cusick, Robert, Wynn, Julia, Chung, Wendy, Mychaliska, George B, Crombleholme, Timothy M, Chung, Dai H, Lim, Foong Yen, Potolka, Douglas, Warner, Brad W, Aspelund, Gundrun, Arkovitz, Marc S
Хэвлэсэн 2015текст -
3
Variants in GATA4 Are a Rare Cause of Familial and Sporadic Congenital Diaphragmatic Hernia -н Yu, Lan, Wynn, Julia, Cheung, Yee Him, Shen, Yufeng, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc S., Chung, Wendy K.
Хэвлэсэн 2012текст -
4
De novo copy number variants are associated with congenital diaphragmatic hernia -н Yu, Lan, Wynn, Julia, Ma, Lijiang, Guha, Saurav, Mychaliska, George B., Crombleholme, Timothy M., Azarow, Kenneth S., Lim, Foong Yen, Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, LeDuc, Charles A., Costa, Katherine, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc, Chung, Wendy K.
Хэвлэсэн 2012текст -
5
Whole Exome Sequencing Identifies de Novo Mutations in GATA6 Associated with Congenital Diaphragmatic Hernia -н Yu, Lan, Bennett, James T., Wynn, Julia, Carvill, Gemma L., Cheung, Yee Him, Shen, Yufeng, Mychaliska, George B., Azarow, Kenneth S., Crombleholme, Timothy M., Chung, Dai H., Potoka, Douglas, Warner, Brad W., Bucher, Brian, Lim, Foong-Yen, Pietsch, John, Stolar, Charles, Aspelund, Gudrun, Arkovitz, Marc S., Mefford, Heather, Chung, Wendy K.
Хэвлэсэн 2014текст -
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The Need for Early Kasai Portoenterostomy: A Western Pediatric Surgery Research Consortium Study -н Kelley-Quon, Lorraine I., Shue, Eveline, Burke, Rita V., Smith, Caitlin, Kling, Karen, Mahdi, Elaa, Ourshalimian, Shadassa, Fenlon, Michael, Dellinger, Matthew, Shew, Stephen B., Lee, Justin, Padilla, Benjamin, Inge, Thomas, Roach, Jonathan, Marwan, Ahmed I., Russell, Katie W., Ignacio, Romeo, Fialkowski, Elizabeth, Nijagal, Amar, Im, Cecilia, Azarow, Kenneth S., Ostlie, Daniel J., Wang, Kasper
Хэвлэсэн 2021текст -
7
Guidelines for Opioid Prescribing in Children and Adolescents After Surgery: An Expert Panel Opinion -н Kelley-Quon, Lorraine I., Kirkpatrick, Matthew G., Ricca, Robert L., Baird, Robert, Harbaugh, Calista M., Brady, Ashley, Garrett, Paula, Wills, Hale, Argo, Jonathan, Diefenbach, Karen A., Henry, Marion C.W., Sola, Juan E., Mahdi, Elaa M., Goldin, Adam B., St Peter, Shawn D., Downard, Cynthia D., Azarow, Kenneth S., Shields, Tracy, Kim, Eugene
Хэвлэсэн 2021текст -
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Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes -н Qiao, Lu, Wynn, Julia, Yu, Lan, Hernan, Rebecca, Zhou, Xueya, Duron, Vincent, Aspelund, Gudrun, Farkouh-Karoleski, Christiana, Zygumunt, Annette, Krishnan, Usha S., Nees, Shannon, Khlevner, Julie, Lim, Foong Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa Ellen, Chung, Dai, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., Soffer, Samuel, Schindel, David, McCulley, David J., Shen, Yufeng, Chung, Wendy K.
Хэвлэсэн 2020текст -
9
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders -н Qi, Hongjian, Yu, Lan, Zhou, Xueya, Wynn, Julia, Zhao, Haoquan, Guo, Yicheng, Zhu, Na, Kitaygorodsky, Alexander, Hernan, Rebecca, Aspelund, Gudrun, Lim, Foong-Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa E., Chung, Dai, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., ElFiky, Mahmoud, Wilson, Jay M., Nickerson, Debbie, Bamshad, Michael, High, Frances A., Longoni, Mauro, Donahoe, Patricia K., Chung, Wendy K., Shen, Yufeng
Хэвлэсэн 2018текст -
10
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene -н Qiao, Lu, Xu, Le, Yu, Lan, Wynn, Julia, Hernan, Rebecca, Zhou, Xueya, Farkouh-Karoleski, Christiana, Krishnan, Usha S., Khlevner, Julie, De, Aliva, Zygmunt, Annette, Crombleholme, Timothy, Lim, Foong-Yen, Needelman, Howard, Cusick, Robert A., Mychaliska, George B., Warner, Brad W., Wagner, Amy J., Danko, Melissa E., Chung, Dai, Potoka, Douglas, Kosiński, Przemyslaw, McCulley, David J., Elfiky, Mahmoud, Azarow, Kenneth, Fialkowski, Elizabeth, Schindel, David, Soffer, Samuel Z., Lyon, Jane B., Zalieckas, Jill M., Vardarajan, Badri N., Aspelund, Gudrun, Duron, Vincent P., High, Frances A., Sun, Xin, Donahoe, Patricia K., Shen, Yufeng, Chung, Wendy K.
Хэвлэсэн 2021текст